Evidence map›Paper›PMID 10378997›Full record

ArticleEnvironmental health perspectives1999

Collection of genomic DNA by buccal swabs for polymerase chain reaction-based biomarker assays.

A H Walker, D Najarian, D L White, J F Jaffe, P A Kanetsky, T R Rebbeck

Registry-linked trialAbstract read
In one paragraph

Article in Environmental health perspectives, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01291745 (Collection of Biological Data With Potential Prognostic Relevance in Patients With MYELODYSPLASTIC SYNDROMES), which is not on this map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01291745 unknown statusnot on this mapstarted 2010, after this paper: background citation

Collection of Biological Data With Potential Prognostic Relevance in Patients With MYELODYSPLASTIC SYNDROMES

TypeobservationalSponsorFondazione Amelia Scorza OnlusRan2010 to 2015Enrolled200ConditionsMyelodysplastic Syndrome
3 · Its place in the literature

Who cites it

55 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. A transdisciplinary model integrating genetic, physiological, and psychological correlates of voluntary exercise.Health psychology : official journal of the Division of Health Psychology, American Psychological Association · 2007
    Trial
  3. Article
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  16. Review
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  19. Relationship of early-onset baldness to prostate cancer in African-American men.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2013
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

A H WalkerDepartment of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics and Cancer Center, University of Pennsylvania School of Medicine, Philadelphia 19104-6021, USA.
D Najarian
D L White
J F Jaffe
P A Kanetsky
T R Rebbeck

Funding

RETINOID IN CHEMOPREVENTION OF PRIMARY MELANOMAP01CA075434 · NCI · UNIVERSITY OF PENNSYLVANIA · PI REBBECK, TIMOTHY R · 1997 to 2000
$935k
ETIOLOGIC HETEROGENEITY IN LATE ONSET BREAST CANCERR01CA073730 · NCI · UNIVERSITY OF PENNSYLVANIA · PI REBBECK, TIMOTHY R · 1997 to 2001
$229k
MOLECULAR EPIDEMIOLOGY OF PROSTATE CANCERR29ES008031 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI REBBECK, TIMOTHY R · 1995 to 1999
–
NCI NIH HHS CA73730NCI NIH HHS CA75434NIEHS NIH HHS ES08031
6 · The paper itself

Abstract

Studies in molecular and genetic epidemiology require a high-throughput, low cost, and reliable means of genomic DNA collection. Buccal (cheek) swabs have been proposed as a means of achieving these goals, but there is little information about the practical application of this approach. From January 1995 to December 1997, we processed 995 buccal swabs for use in polymerase chain reaction (PCR)-based genotype assays in the context of ongoing molecular epidemiologic studies. Six hundred forty-seven of these swabs were processed immediately after collection and 348 were received by mail. We were able to obtain at least one genotype from 99.7% (645 of 647) of fresh-processed and 97.4% (330 of 339) of mailed biosamples. A PCR success rate of 90.3% (2,546 genotypes from 2,819 assays) was achieved. Genotypes were obtained from 96.1% (1, 865 genotypes from 1,941 assays) of fresh-processed biosamples and 77.6% (681 genotypes from 878 assays) of mailed biosamples. PCR success rates at any single locus ranged from 92.6 to 98.8% (fresh-processed) and 75.5 to 79.6% (mailed). The PCR success rate among fresh-processed biosamples was significantly higher than among mailed biosamples (Fisher's exact test p < 0.0001), and more attempts were required to obtain a successful PCR result for mailed biosamples as compared to fresh-processed biosamples. For one locus (CYP3A4), a subset of mailed biosamples was purified if two or more PCR failures occurred. Additional genotypes were obtained in 58.3% of these previously failed biosamples. Time from biosample receipt to DNA extraction had no effect on PCR success. After storage of processed biosamples for as long as 3 years, there was no appreciable decrease in the rate of PCR success. These results suggest that adequate DNA for PCR-based applications can be obtained from buccal swabs, but sampling or processing considerations may be important in obtaining optimal results.

Indexed as

Polymerase Chain ReactionSpecimen HandlingAdultAgedAged, 80 and overBiomarkersCheekDNAHumansMiddle AgedMouth MucosaTime FactorsBiomarkersDNA

Identifiers

PMID10378997
PMCPMC1566681

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.